NM_002180.3(IGHMBP2):c.1143C>T (p.Leu381=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 18, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000600634.2
Allele description [Variation Report for NM_002180.3(IGHMBP2):c.1143C>T (p.Leu381=)]
NM_002180.3(IGHMBP2):c.1143C>T (p.Leu381=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 12, 2024